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Disease Ontology Browser
X-linked cone-rod dystrophy 1 (DOID:0111008)
Alliance: disease page
Synonyms: COD1; CORDX1; X-linked cone dystrophy 1
Alt IDs: OMIM:304020
Definition: A cone-rod dystrophy that has_material_basis_in mutation in an alternative terminal exon 15 of the RPGR gene on chromosome Xp11.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
01/18/2022
MGI 6.17
The Jackson Laboratory